Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Divisions of Pulmonary, Critical Care and Sleep Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Int J Mol Sci. 2020 Oct 29;21(21):8081. doi: 10.3390/ijms21218081.
The 1918 influenza killed approximately 50 million people in a few short years, and now, the world is facing another pandemic. In December 2019, a novel coronavirus named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused an international outbreak of a respiratory illness termed coronavirus disease 2019 (COVID-19) and rapidly spread to cause the worst pandemic since 1918. Recent clinical reports highlight an atypical presentation of acute respiratory distress syndrome (ARDS) in COVID-19 patients characterized by severe hypoxemia, an imbalance of the renin-angiotensin system, an increase in thrombogenic processes, and a cytokine release storm. These processes not only exacerbate lung injury but can also promote pulmonary vascular remodeling and vasoconstriction, which are hallmarks of pulmonary hypertension (PH). PH is a complication of ARDS that has received little attention; thus, we hypothesize that PH in COVID-19-induced ARDS represents an important target for disease amelioration. The mechanisms that can promote PH following SARS-CoV-2 infection are described. In this review article, we outline emerging mechanisms of pulmonary vascular dysfunction and outline potential treatment options that have been clinically tested.
1918 年流感在短短几年内导致约 5000 万人死亡,而如今,世界正面临另一场大流行。2019 年 12 月,一种名为严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的新型冠状病毒引发了一种名为 2019 年冠状病毒病(COVID-19)的呼吸道疾病国际暴发,并迅速传播,造成自 1918 年以来最严重的大流行。最近的临床报告强调了 COVID-19 患者急性呼吸窘迫综合征(ARDS)的非典型表现,其特征为严重低氧血症、肾素-血管紧张素系统失衡、血栓形成过程增加和细胞因子释放风暴。这些过程不仅会加重肺损伤,还会促进肺血管重塑和血管收缩,这是肺动脉高压(PH)的标志。PH 是 ARDS 的并发症,但一直未受到重视;因此,我们假设 COVID-19 诱导的 ARDS 中的 PH 是疾病改善的重要靶点。描述了可以促进 SARS-CoV-2 感染后 PH 的机制。在这篇综述文章中,我们概述了肺血管功能障碍的新兴机制,并概述了已在临床上测试过的潜在治疗选择。